Qc Salary at Micro Molding Inc BETA

QC Analyst 3 Job Title: Quality Control Laboratory Analyst 3 – Radiopharmaceuticals About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company beginning operations in Springfield, NJ. The state-of-the-art facility will provide contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. Evergreen is a small team, where all team members support each other in a variety of activities. Job Description: We are looking for an experienced and proactive Quality Control Laboratory Analyst 3 to join our team. In this role, the candidate will participate in critical quality control processes for our radiopharmaceutical products, ensuring all operations comply with stringent industry standards and regulatory guidelines. The ideal candidate will have significant experience in pharmaceutical or radiopharmaceutical environments, a strong background in analytical techniques, and the ability to troubleshoot

QC Analyst 2 Job Title: Quality Control Laboratory Analyst 2 – Radiopharmaceuticals About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company beginning operations in Springfield, NJ. The state-of-the-art facility will provide contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. The company expects rapid growth in the next few years. Evergreen is a small team, where all team members support each other in a variety of activities. Job Description: We are seeking a highly motivated and detail-oriented Quality Control Laboratory Analyst 2 to join our team. This individual will play a key role in ensuring the highest standards of quality and compliance in our radiopharmaceutical release processes. The ideal candidate will have a background in pharmaceutical or life sciences, and hands-on experience with analytical techniques such as GC (Gas Chromatography), TLC (Thin Layer Chromatography

Our client is actively looking for a QC Stability Program Manager for their growing team. This is an on-site position in Cranbury NJ. You should apply if you have: B.S. with 6+ years of QC lab experience in an FDA regulated environment(Pharma preferred) Management and/or project management experience Experience leading/owning stability programs Experience overseeing analytical testing and validation processes

Job Description Job Description Position Summary: This position will report to quality management (QA/QC Manager). The QC Data Reviewer will be responsible for review of various data and documentations generated by Quality control department as per cGMP and company procedures. The QC Data Reviewer will meet departmental, company, and Quality goals by accomplishing the following responsibilities: Essential functions and Responsibilities: Quality review of QC lab generated data and documentation for accuracy, completeness, and compliance in timely manner. Audit trails review of analytical instrumentation to ensure data integrity. Raw data note book review for documented information such as calculation verification, standard/sample preparation, reagent preparation, instrument calibration, reagent expires, logbook entries, control charts, etc. Facilitates laboratory data or documentation corrections with analysts to ensure accuracy. Must have a working knowledge of the analytical instrumen

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . At Bristol Myers Squibb we are reimagining the future of cell t

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . At **Bristol Myers Squibb** we are reimagining the future of ce

Job Description Job Description Job Title: Project Manager (QC) Location: Princeton, NJ Job Type: Full-Time Skills Required: · Strong background in building construction. · Expertise in quality control (QC) processes and procedures. · Knowledge of construction industry standards, codes, and regulations. · Experience in project planning, execution, and quality assurance. · Proficiency in construction management software. · Strong problem-solving and analytical skills. · Ability to manage multiple projects and ensure compliance with QC standards. · Excellent communication and leadership abilities. · Experience conducting site inspections and audits. · Attention to detail and ability to document QC processes effectively. Company Description JCMS, Inc. is headquartered in Mercerville, New Jersey with office in New York. We have over eighty five employees on our full time staff in various disciplines. They are cost estimators, cost and scheduling engineers, document control specialists, off

Job Type Full-time Description The QC Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial small molecule and biosimilar products in cGMP-compliant laboratories. A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required. Analytical testing to support product in-process, release, and stability programs. Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance. Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans. Work with cross-functional teams to advance projects, maintain equipment, and author